Aionex, Inc.

Form 483

Madison, Tennessee, United StatesFEI 3005627440Issued July 02, 2013

View FDA's Record for This Firm

Source: FDA inspection record. Confirmed against FDA's published inspection data for this establishment and inspection date. FDA has published the inspection and what it cited, but not the form itself, which usually takes six to twelve months. To check it, open FDA's record for this establishment on FDA's Data Dashboard, listed under FEI 3005627440.

Observations10

Issue DateJuly 02, 2013

StatusNo Warning Letter

Related Inspections6

Establishment Details

Firm: Aionex, Inc.
Location: Madison, Tennessee, United States
FEI Number: 3005627440
Product Type: Devices
Issue Date: July 02, 2013
Country: United States

Inspection History, 2012 to 2026

NAI4

VAI1

OAI1

NAI means No Action Indicated. VAI means Voluntary Action Indicated. OAI means Official Action Indicated.

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Aionex, Inc. FDA Form 483, Madison, Tennessee, July 2, 2013